rs10773771
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10773771(C;C) |
Make rs10773771(C;T) |
Make rs10773771(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 130371771 |
Gene | PIWIL1 |
is a | snp |
is | mentioned by |
dbSNP | rs10773771 |
dbSNP (classic) | rs10773771 |
ClinGen | rs10773771 |
ebi | rs10773771 |
HLI | rs10773771 |
Exac | rs10773771 |
Gnomad | rs10773771 |
Varsome | rs10773771 |
LitVar | rs10773771 |
Map | rs10773771 |
PheGenI | rs10773771 |
Biobank | rs10773771 |
1000 genomes | rs10773771 |
hgdp | rs10773771 |
ensembl | rs10773771 |
geneview | rs10773771 |
scholar | rs10773771 |
rs10773771 | |
pharmgkb | rs10773771 |
gwascentral | rs10773771 |
openSNP | rs10773771 |
23andMe | rs10773771 |
SNPshot | rs10773771 |
SNPdbe | rs10773771 |
MSV3d | rs10773771 |
GWAS Ctlg | rs10773771 |
GMAF | 0.4982 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23868705] Potentially functional genetic variants in microRNA processing genes and risk of HBV-related hepatocellular carcinoma
[PMID 24255581] Genetic variants in RAN, DICER and HIWI of microRNA biogenesis genes and risk of cervical carcinoma in a Chinese population